FT-011
CAS No. 1001288-58-9
FT-011 ( FT011 | SHP-627 )
产品货号. M10013 CAS No. 1001288-58-9
一种新型抗纤维化剂,可防止培养的肾系膜细胞中 TGF-β 刺激的胶原蛋白产生(30 uM 时抑制 55-70%)。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 5MG | ¥316 | 有现货 |
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| 10MG | ¥518 | 有现货 |
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| 25MG | ¥996 | 有现货 |
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| 50MG | ¥1847 | 有现货 |
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| 100MG | ¥3013 | 有现货 |
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| 200MG | ¥4188 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称FT-011
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述一种新型抗纤维化剂,可防止培养的肾系膜细胞中 TGF-β 刺激的胶原蛋白产生(30 uM 时抑制 55-70%)。
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产品描述A novel anti-fibrotic agent that prevents TGF-beta-stimulated production of collagen in cultured renal mesangial cells (55-70% inhibition at 30 uM); inhibits both TGF-β1 and PDGF-BB induced collagen production as well as PDGF-BB-mediated mesangial proliferation, attenuates the decline in GFR, proteinuria and glomerulosclerosis in a robust model of non-diabetic kidney disease; attenuates fibrosis and chronic heart failure in experimental diabetic cardiomyopathy.(In Vivo):FT011 (100 mg/kg b.i.d., p.o., for 4 weeks) improves the cardiac function and and myocardial remodeling in myocardial infarction rats.
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体外实验——
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体内实验FT011 (100 mg/kg b.i.d., p.o., for 4 weeks) improves the cardiac function and and myocardial remodeling in myocardial infarction rats. Animal Model:Seventy male Sprague Dawley (SD) rats (weighing 200-250 g)Dosage:100 mg/kg Administration:B.I.D., p.o. on day 7 after surgery, for 4 weeks Result:Increased ejection fraction, fraction shortening and preload recruitable stroke work.
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同义词FT011 | SHP-627
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通路TGF-beta/Smad
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靶点TGFBR
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受体TGFBR
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研究领域Other Indications
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适应症Other Disease
化学信息
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CAS Number1001288-58-9
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分子量351.3527
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分子式C20H17NO5
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纯度>98% (HPLC)
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溶解度DMSO: ≥ 29 mg/mL
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SMILESO=C(O)C1=CC=CC=C1NC(/C=C/C2=CC=C(OCC#C)C(OC)=C2)=O
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化学全称Benzoic acid, 2-[[(2E)-3-[3-methoxy-4-(2-propyn-1-yloxy)phenyl]-1-oxo-2-propen-1-yl]amino]-
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Zammit SC, et al. Bioorg Med Chem Lett. 2009 Dec 15;19(24):7003-6.
2. Zhang Y, et al. Eur J Heart Fail. 2012 May;14(5):549-62.
3. Gilbert RE, et al. PLoS One. 2012;7(10):e47160.
4. Deliyanti D, et al. PLoS One. 2015 Jul 29;10(7):e0134392.
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